Vesper Bio announces positive Phase Ib/IIa topline results for lead candidate VES001 for frontotemporal degeneration

Mads Kjolby, Co-Founder and Chief Medical Officer at Vesper Bio, said: "Progranulin is vital for maintaining neuronal health. However, progranulin levels in asymptomatic people with GRN mutations are typically half that of people without such mutations. Based on these topline Phase Ib/IIa data, we believe VES001 has the potential to normalise progranulin levels not only in asymptomatic individuals with GRN mutations, but in symptomatic people too, without affecting other sortilin functions crucial for neuronal health. We therefore think VES001 has great potential to slow or even arrest FTD-GRN disease progression."

COPENHAGEN, Denmark, 31/10/2025 (informazione.news - comunicati stampa - salute e benessere)

 

 

The open-label, single arm study included six individuals from the Netherlands and the UK who all carry GRN mutations, which cause them to have very low progranulin levels, but are asymptomatic. The study demonstrated that VES001 had a safe and tolerable profile. It also confirmed target engagement took place, with significantly elevated levels of progranulin in both plasma and CSF found in the participants after treatment, compared to baseline levels of the protein for this population. The findings provide the first validation of Vesper's approach of restoring normal progranulin levels in this population by selectively inhibiting progranulin binding to the sortilin receptor without affecting sortilin levels or functions important for neuronal health. This is in contrast to antibody-mediated degradation of sortilin.

The study has been carried out at two clinical centres: the Erasmus University Medical Centre, Rotterdam , in the Netherlands , and the Leonard Wolfson Experimental Neurology Centre Clinical Research Facility at the National Hospital for Neurology and Neurosurgery, University College London, in the UK.

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Participants in the PhIb/IIa SORT-IN-2 study received daily oral doses of VES001 – first at a lower dose for 28 days, and then at a higher dose for 56 days. VES001 was well tolerated with only a few mild adverse events (AEs) reported. There were no severe adverse events (SAEs) reported, or discontinuations due to treatment-related effects.

Separately, Vesper Bio is pleased to announce that it has successfully completed its long-term, pivotal toxicology studies of VES001 in animals.

The SORT-IN-2 study is supported by the Alzheimer's Drug Discovery Foundation (ADDF) and the Association for Frontotemporal Degeneration (AFTD) through the TreatFTD programme. It will fully report in Q1 2026. Vesper Bio will then prepare to start a Phase IIb/III clinical trial to evaluate VES001's efficacy on clinical progression and biomarker endpoints in symptomatic FTD-GRN patients.

For more information about the trial (NCT06705192), please visit www.clinicaltrials.gov.  

Vesper Bio is a clinical stage biotech and world leader in sortilin receptor biology. Vesper is developing small molecule-based selective sortilin inhibitors as novel oral therapies for neurodegenerative and neuropsychiatric diseases. VES001, its lead compound, is a patient friendly, first-in-class, brain penetrant, oral treatment which targets progranulin deficiency, a major underlying cause of a genetically driven type of frontotemporal degeneration (FTD-GRN). VES001 is a competitive sortilin inhibitor that selectively prevent degradation of progranulin while preserving sortilin levels and functions crucial for neuronal health, in contrast to antibody-mediated degradation of sortilin. With VES001, Vesper aims at normalising levels of progranulin and reducing neuroinflammation and disease progression in both asymptomatic and symptomatic FTD-GRN patients.

Frontotemporal degeneration (FTD), also known as frontotemporal lobar degeneration (FTLD), is a group of brain disorders that cause degeneration in the frontal and temporal lobes of the brain. FTD impacts a person's behaviour, judgement, communication and ability to participate in all activities of daily living. It is the most common cause of dementia in people under the age of 60 and is often misdiagnosed as Alzheimer's disease. FTD-GRN is a form of FTD caused by mutations of the progranulin gene (GRN), resulting in low progranulin levels. FTD-GRN is thought to account for a quarter of familial FTD cases.

For further information please visit, https://www.vesperbio.com/

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